CA1142291A - Process for preparing bimodal or multimodal polymers of conjugated dienes - Google Patents
Process for preparing bimodal or multimodal polymers of conjugated dienesInfo
- Publication number
- CA1142291A CA1142291A CA000375137A CA375137A CA1142291A CA 1142291 A CA1142291 A CA 1142291A CA 000375137 A CA000375137 A CA 000375137A CA 375137 A CA375137 A CA 375137A CA 1142291 A CA1142291 A CA 1142291A
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- CA
- Canada
- Prior art keywords
- conjugated diene
- fact
- process according
- reaction
- alkyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F36/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
- C08F36/02—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
- C08F36/04—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated
Abstract
ABSTRACT OF THE DISCLOSURE:
A process of preparing a bimodal or multimodal homopolymer of a conjugated diene or a bimodal or multi-modal copolymer of a conjugated diene with another conjugated diene or with a vinyl aromatic compound consists in polymer-izing the monomer(s) in a reaction medium at a temperature of between 20°C. and 200°C. in the presence of a catalyst system formed of the reaction product of:
(a) an organic compound of a metal of group 3A
of the periodic classification of elements of the Mendeleev Table having one of the following formulas:
M2(M3R1R2R3R4)2 with (b) at least one electron-donor compound containing at least one heteroatom, and adding hydrogen as a modifying agent to the reaction medium during the course of the polymerization reaction.
A process of preparing a bimodal or multimodal homopolymer of a conjugated diene or a bimodal or multi-modal copolymer of a conjugated diene with another conjugated diene or with a vinyl aromatic compound consists in polymer-izing the monomer(s) in a reaction medium at a temperature of between 20°C. and 200°C. in the presence of a catalyst system formed of the reaction product of:
(a) an organic compound of a metal of group 3A
of the periodic classification of elements of the Mendeleev Table having one of the following formulas:
M2(M3R1R2R3R4)2 with (b) at least one electron-donor compound containing at least one heteroatom, and adding hydrogen as a modifying agent to the reaction medium during the course of the polymerization reaction.
Description
~22~
The object of the present invention is a process which makes it possible to modify the molecular weight distribution upon the synthesis of a homopolymer of a con-jugated diene or a copolymer of a conjugated diene with another conjugated diene or with a vinyl aromatic compound.
From West German patent application No. 26 07 721 (which corresponds to U.S. patents Nos. 4,110,525, 4,112,210, 4,148,985, 4,148,986 and 4,152,505) it is known to prepare a homopolymer of a conjugated diene or a copolymer of a conjugated diene with another conjugated diene or with a vinyl aromatic compound having extremely different microstruc-tures and a mono~odal distribution of the molecular weights by means of a catalyst system formed of the reaction product of:
. ~a) an organic compound of a metal of group 3A
of the periodic classification of elements of the Mendeleev Table having one of the following formulas:
MlM3RlR2R3R4 : ~ : M2 (M3RlR2R3R4 ) 2 ~: 20 M3RlR R
MloM3RlR2 in which Ml represents an alkali metal, M represents an alkaline earth metal, M3 represents a metal of group 3A, Rl, R2, R3 represent an alkyl or aralkyl radical and R4 represents either an alkyl or aralkyl radical or a radical ; XB in which X represents an oxygen, sulfur or nitrogen atom and B is an alkyl or aralkyl radical or a radical M3~R5R6) in which R , R6 represent an alkyl or aralkyl radical, with (b) at least one electron-donor compound containing at least one heteroatom selected from the group consisting of aprotic polar compounds, protic polar compounds and compounds formed of the reaction products of protic polar .. ~.
- -l~ZZ91 compounds with an alkali metal or with an alkaline earth metal.
It is desirable to have means which make it possible to modify and regulate the distribution of the molecular weights of the homopolymerofa conjugated diene or a copolymer of a conjugated diene with another conjugated diene or with a vinyl aromatic compound for a number of industrial uses of these products, since the modification of the molecular weight distribution makes it possible to improve greatly certain properties such as, for instance, the machine-ability, the cold flow, the raw coherence, the raw tackiness,etc., without penalizing the other properties.
It is known to the man skilled in the art that it is possible to broaden the molecular weight distribution and obtain bimodal or multimodal polymers by mixing together several polymers of different viscosity.
However, such a process has the drawback of requiring the separate synthesis of several polymers of different viscosities, which results in problems of reproducibility of the process, requires very large quantities of catalyst, results in long periods of time and finally makes this process uninteresting both from a technical standpoint and from an economic standpoint.
It is also known to modify the molecular weight distribution of homopolymers and copolymers in processes carried out either batchwise or continuously by breaking up the amount of catalyst necessary and adding it at different times during the course of the homopolymerization or copolymer-ization. However, such a manner of operation, which also requires very large amounts of catalyst, which are larger the greater the desired broadening of the molecular weight distribution is, is therefore also very expensive. Furthermore, it would be extremely difficult to carry out industrially.
~1~2~1 The object of the present invention is to remedy these drawbacks by providing a process which is economically more interesting and which makes it possible easily to modify and regulate the molecular weight distribution during the course of the synthesis of a homopolymer of a conjugated diene or a copolymer of a conjugated diene with another conjugated diene or with a vinyl aromatic compound and to obtain a bimodal or multimodal homopolymer or copolymer.
The applicant has unexpectedly found that it is possible to achieve this purpose when the homopolymerization of the conjugated diene or the copolymerization of the conjugated diene with another conjugated diene or with a vinyl aromatic compound by the use of the catalyst systems described above is effected in the presence of a modifying agent which is not a polymerization initiator.
Thus, the present inventlon concerns a process of preparing a homopolymer of a conjugated diene or a copolymer of a conjugated diene with another conjugated diene or with a vinyl aromatic compound, whether bimodal or multimodal, which consists in polymerizing the monomer~s) in a reaction medium at a temperature of between 20C. and 200C. in the presence of a catalyst system formed of the reaction product of:
(a) an organic compound of a metal of group 3A
of the periodic classification of elements of the Mendeleev Table having one of the following formulas:
MlM3RlR2R3R4 M2(M3RlR2R3R4) M R R R
MloM3R R
in which Ml represents an alkali metal, M2 represents an alkaline earth metal, M3 represents a metal of group 3A, R , R2, R3 represent an alkyl or aralkyl radical and R represents ~ ~` ~
1~2Z~3~
either an alkyl or aralkyl radical or a radical XB in which X
represents an oxygen, sulfur or nitrogen atom and B represents an alkyl or aralkyl radical or a radical M (P~5R6) in which R5, R6 represent an alkyl or aralkyl radical, with (b) at least one electron-donor compound containing at least one heteroatom selected from the group consisting of aprotic polar compounds, protic polar compounds and compounds formed of the reaction products of protic polar compounds with an alkali metal or with an alkaline earth metal, characterized by adding hydrogen as a modifying agent to the reaction medium during the course of the polymerization reaction.
The periodic classification of elements of the Mendeleev Table referred to herein is that given in the 59th edition of the " Handbook of Chemistry and Physics" .
This process makes it possible to modify the molecular weight distribution as desired and to obtain improved proper-ties of raw tackiness, raw coherence and machineability without requirlng additional amounts of catalyst and without, at the same time, penalizing the other properties.
The process of the invention makes it possible to obtain homopolymers and copolymers having bimodal or multimodal moIecular weight distributions. The fraction or fractions obtained after addition of the modifying agent are of low .
molecular weight. Furthermore, the average molecular weights of said fraction or fractions of low molecular weight as well as the quantity of these low molecular weights are a function of the amount of the modifying agent added and of the time when this modifying agent is added during the course of the polymer-ization reaction.
By selecting the amount to be added and the time of the addition as a function of the percentage of conversion of the monomers at the time in question as compared with the final conversion percentage, it is possible to prepare bimodal or multimodal homopolymers and copolymers, the quantity of the high and low molecular weights of which as well as the respec-tive average molecular weights of these high and low molecular weights can be regulated as desired.
It is desirable to use amounts of hydrogen solubilized in the reaction medium of between 0.1 and 100 ppm. The larger the amount of solubilized hydrogen, the lower the molecular weight of the low molecular weights will be.
The hydrogen is added during the course of the polymerization reaction and preferably when the conversion of the monomers is between 20% and 90%. The polymerization process can be conducted in bulk or in solution ina hydrocarbon sol-vent either batchwise or continuously. In the latter case, one operates in two or more reactors placed in series at identical or different polymerization temperatures. Depending on the extent of the effect desired, the hydrogen is added in one or more portions.
In the polymerization process of the invention aliphatic soIvents, such as hexane and heptane, or aromatic solvents, such as benzene and toluene, can be used as a hydrocarbon solvent.
The organometallic compounds of a metal of group 3A which are particularly suitable as components of the catalyst system are those in which the group 3A metal is boron, aluminum, gallium, indium and thallium and those in which the alkali metal is lithium, sodium or potassium and those in which the alkaline earth metal is magnesium, calcium, stron-tium or barium. For example, the following compound may be mentioned:
Al(CH3)3~ Al(C2H5)3~ Al(i - C4Hg ) 3, Li ~l(C2H5) 4 114Z~l ~Al(C2 5)47~ K~Al(c2Hs)47, Li~Al(C2H5)3O C2H57, Li~Al(C2H5)3 Al(C2H5)27, MgrAl(C2H5)4~2, C2 5 g 2 5 4 rAl(C2H5) ~ 2' Sr~Al(C2H5)4~2, Ba~Al(c2H5)4~2, L~l(C2Hs)3 C2H5~2~ Ba~al - (iso C4Hg)4~2~
( 2 5)2~ Na O Al(C2H5)2, B(CH3)3, g(c2H ) ( 2 5)4~ Li B(C2H5)3C4Hg, Ga(C2H5)3, In(C2H5)3~ Tl(C2 5 3 As aprotic polar compounds there are particularly suitable the ethers and particularly the cyclic ethers, such as tetrahydrofuran and dioxane, and the corresponding thio-ethers, the tertiary amines such as N,N,N',N'-tetramethyl-ethylene-diamine, the aromatic amines and, in particular, the derivatives of pyridine and the corresponding oxides, the phosphorus compounds such as phosphines and their oxides, the phosphites, the phosphoroamides and, in particular, hexamethylphosphorotriamide, the ketones and particularly acetone, the nitriles and particularIy acetonitrile, the aldehydes, the esters, the amides, the nitroaliphatic or aromatic compounds, the sulfoxides and particularly dimethyl-sulfoxide,the sulfones and the sulfites.
As protic polar compounds there are suitable, in particular, water, the alcohols and particularly methanol, theprimary or secondary amines and the thiols.
As compounds formed of the reaction products of protic polar compounds with an alkali metalor with an alkaline earth metal there are particularly suitable the alcoholates and the phenates of an alkali metal or alkaline earth metal, the alkali metal or alkaline earth mercapto- and thio-phenates as well as the ether-alcoholate and amine-alcoholate compounds.
The process of the invention is particularly suitable for the homopolymerization of a conjugated diene or the copolymerization of a conjugated diene with another `~i4Z~
conj~lgated diene or with a vinyl aromatic compound.
As representative examples of conjugated dienes there are suitable, in particular, butadiene-1,3, isoprene,
The object of the present invention is a process which makes it possible to modify the molecular weight distribution upon the synthesis of a homopolymer of a con-jugated diene or a copolymer of a conjugated diene with another conjugated diene or with a vinyl aromatic compound.
From West German patent application No. 26 07 721 (which corresponds to U.S. patents Nos. 4,110,525, 4,112,210, 4,148,985, 4,148,986 and 4,152,505) it is known to prepare a homopolymer of a conjugated diene or a copolymer of a conjugated diene with another conjugated diene or with a vinyl aromatic compound having extremely different microstruc-tures and a mono~odal distribution of the molecular weights by means of a catalyst system formed of the reaction product of:
. ~a) an organic compound of a metal of group 3A
of the periodic classification of elements of the Mendeleev Table having one of the following formulas:
MlM3RlR2R3R4 : ~ : M2 (M3RlR2R3R4 ) 2 ~: 20 M3RlR R
MloM3RlR2 in which Ml represents an alkali metal, M represents an alkaline earth metal, M3 represents a metal of group 3A, Rl, R2, R3 represent an alkyl or aralkyl radical and R4 represents either an alkyl or aralkyl radical or a radical ; XB in which X represents an oxygen, sulfur or nitrogen atom and B is an alkyl or aralkyl radical or a radical M3~R5R6) in which R , R6 represent an alkyl or aralkyl radical, with (b) at least one electron-donor compound containing at least one heteroatom selected from the group consisting of aprotic polar compounds, protic polar compounds and compounds formed of the reaction products of protic polar .. ~.
- -l~ZZ91 compounds with an alkali metal or with an alkaline earth metal.
It is desirable to have means which make it possible to modify and regulate the distribution of the molecular weights of the homopolymerofa conjugated diene or a copolymer of a conjugated diene with another conjugated diene or with a vinyl aromatic compound for a number of industrial uses of these products, since the modification of the molecular weight distribution makes it possible to improve greatly certain properties such as, for instance, the machine-ability, the cold flow, the raw coherence, the raw tackiness,etc., without penalizing the other properties.
It is known to the man skilled in the art that it is possible to broaden the molecular weight distribution and obtain bimodal or multimodal polymers by mixing together several polymers of different viscosity.
However, such a process has the drawback of requiring the separate synthesis of several polymers of different viscosities, which results in problems of reproducibility of the process, requires very large quantities of catalyst, results in long periods of time and finally makes this process uninteresting both from a technical standpoint and from an economic standpoint.
It is also known to modify the molecular weight distribution of homopolymers and copolymers in processes carried out either batchwise or continuously by breaking up the amount of catalyst necessary and adding it at different times during the course of the homopolymerization or copolymer-ization. However, such a manner of operation, which also requires very large amounts of catalyst, which are larger the greater the desired broadening of the molecular weight distribution is, is therefore also very expensive. Furthermore, it would be extremely difficult to carry out industrially.
~1~2~1 The object of the present invention is to remedy these drawbacks by providing a process which is economically more interesting and which makes it possible easily to modify and regulate the molecular weight distribution during the course of the synthesis of a homopolymer of a conjugated diene or a copolymer of a conjugated diene with another conjugated diene or with a vinyl aromatic compound and to obtain a bimodal or multimodal homopolymer or copolymer.
The applicant has unexpectedly found that it is possible to achieve this purpose when the homopolymerization of the conjugated diene or the copolymerization of the conjugated diene with another conjugated diene or with a vinyl aromatic compound by the use of the catalyst systems described above is effected in the presence of a modifying agent which is not a polymerization initiator.
Thus, the present inventlon concerns a process of preparing a homopolymer of a conjugated diene or a copolymer of a conjugated diene with another conjugated diene or with a vinyl aromatic compound, whether bimodal or multimodal, which consists in polymerizing the monomer~s) in a reaction medium at a temperature of between 20C. and 200C. in the presence of a catalyst system formed of the reaction product of:
(a) an organic compound of a metal of group 3A
of the periodic classification of elements of the Mendeleev Table having one of the following formulas:
MlM3RlR2R3R4 M2(M3RlR2R3R4) M R R R
MloM3R R
in which Ml represents an alkali metal, M2 represents an alkaline earth metal, M3 represents a metal of group 3A, R , R2, R3 represent an alkyl or aralkyl radical and R represents ~ ~` ~
1~2Z~3~
either an alkyl or aralkyl radical or a radical XB in which X
represents an oxygen, sulfur or nitrogen atom and B represents an alkyl or aralkyl radical or a radical M (P~5R6) in which R5, R6 represent an alkyl or aralkyl radical, with (b) at least one electron-donor compound containing at least one heteroatom selected from the group consisting of aprotic polar compounds, protic polar compounds and compounds formed of the reaction products of protic polar compounds with an alkali metal or with an alkaline earth metal, characterized by adding hydrogen as a modifying agent to the reaction medium during the course of the polymerization reaction.
The periodic classification of elements of the Mendeleev Table referred to herein is that given in the 59th edition of the " Handbook of Chemistry and Physics" .
This process makes it possible to modify the molecular weight distribution as desired and to obtain improved proper-ties of raw tackiness, raw coherence and machineability without requirlng additional amounts of catalyst and without, at the same time, penalizing the other properties.
The process of the invention makes it possible to obtain homopolymers and copolymers having bimodal or multimodal moIecular weight distributions. The fraction or fractions obtained after addition of the modifying agent are of low .
molecular weight. Furthermore, the average molecular weights of said fraction or fractions of low molecular weight as well as the quantity of these low molecular weights are a function of the amount of the modifying agent added and of the time when this modifying agent is added during the course of the polymer-ization reaction.
By selecting the amount to be added and the time of the addition as a function of the percentage of conversion of the monomers at the time in question as compared with the final conversion percentage, it is possible to prepare bimodal or multimodal homopolymers and copolymers, the quantity of the high and low molecular weights of which as well as the respec-tive average molecular weights of these high and low molecular weights can be regulated as desired.
It is desirable to use amounts of hydrogen solubilized in the reaction medium of between 0.1 and 100 ppm. The larger the amount of solubilized hydrogen, the lower the molecular weight of the low molecular weights will be.
The hydrogen is added during the course of the polymerization reaction and preferably when the conversion of the monomers is between 20% and 90%. The polymerization process can be conducted in bulk or in solution ina hydrocarbon sol-vent either batchwise or continuously. In the latter case, one operates in two or more reactors placed in series at identical or different polymerization temperatures. Depending on the extent of the effect desired, the hydrogen is added in one or more portions.
In the polymerization process of the invention aliphatic soIvents, such as hexane and heptane, or aromatic solvents, such as benzene and toluene, can be used as a hydrocarbon solvent.
The organometallic compounds of a metal of group 3A which are particularly suitable as components of the catalyst system are those in which the group 3A metal is boron, aluminum, gallium, indium and thallium and those in which the alkali metal is lithium, sodium or potassium and those in which the alkaline earth metal is magnesium, calcium, stron-tium or barium. For example, the following compound may be mentioned:
Al(CH3)3~ Al(C2H5)3~ Al(i - C4Hg ) 3, Li ~l(C2H5) 4 114Z~l ~Al(C2 5)47~ K~Al(c2Hs)47, Li~Al(C2H5)3O C2H57, Li~Al(C2H5)3 Al(C2H5)27, MgrAl(C2H5)4~2, C2 5 g 2 5 4 rAl(C2H5) ~ 2' Sr~Al(C2H5)4~2, Ba~Al(c2H5)4~2, L~l(C2Hs)3 C2H5~2~ Ba~al - (iso C4Hg)4~2~
( 2 5)2~ Na O Al(C2H5)2, B(CH3)3, g(c2H ) ( 2 5)4~ Li B(C2H5)3C4Hg, Ga(C2H5)3, In(C2H5)3~ Tl(C2 5 3 As aprotic polar compounds there are particularly suitable the ethers and particularly the cyclic ethers, such as tetrahydrofuran and dioxane, and the corresponding thio-ethers, the tertiary amines such as N,N,N',N'-tetramethyl-ethylene-diamine, the aromatic amines and, in particular, the derivatives of pyridine and the corresponding oxides, the phosphorus compounds such as phosphines and their oxides, the phosphites, the phosphoroamides and, in particular, hexamethylphosphorotriamide, the ketones and particularly acetone, the nitriles and particularIy acetonitrile, the aldehydes, the esters, the amides, the nitroaliphatic or aromatic compounds, the sulfoxides and particularly dimethyl-sulfoxide,the sulfones and the sulfites.
As protic polar compounds there are suitable, in particular, water, the alcohols and particularly methanol, theprimary or secondary amines and the thiols.
As compounds formed of the reaction products of protic polar compounds with an alkali metalor with an alkaline earth metal there are particularly suitable the alcoholates and the phenates of an alkali metal or alkaline earth metal, the alkali metal or alkaline earth mercapto- and thio-phenates as well as the ether-alcoholate and amine-alcoholate compounds.
The process of the invention is particularly suitable for the homopolymerization of a conjugated diene or the copolymerization of a conjugated diene with another `~i4Z~
conj~lgated diene or with a vinyl aromatic compound.
As representative examples of conjugated dienes there are suitable, in particular, butadiene-1,3, isoprene,
2,3-dimethyl-butadiene-1,3, pentadiene-1,3, 2-methyl-pentadiene-1,3 and 2,4-hexadiene.
As representative examples of vinyl aromatic com-pounds there are suitable, in particular, styrene, ortho-, meta- and para-methylstyrene, " vinyl toluene" , the di-and poly-methylstyrenes, p-tertiobutylstyrene, the vinyl naphthalenes, the methoxystyrenes, the halostyrenes, vinyl mesitylene and divinyl benzene.
The following nonllmitative examples are given by way of illustration of the invention. In these examples, the inherent viscosities are established at 25C. in a 1 g./liter solution in toluene; the concentrations of compounds constitut-ing the catalyst system are expressed in micromols per 100 g.
of monomers. The percentages of 1,2 and trans linkages are expressed with respect to the polybutadiene portion and the percentage of styrene is expressed with respect to the total amount of copolymer obtained.
The time elapsed between the start of the polymer-ization reaction and the moment when the modifying agent is added is designated ln the examples as " elapsed time" and the percentage of conversion reached at the time of the ad-dition of the modifying agent is designated by " % conv."
The figures of the drawing show the distribution of the molecular weights of the homopolymers obtained at the end of the polymerization reaction which was obtained by gel permeation chromatography. The molecular weights are shown on the abscissa and the refraction index difference ~i on the ordinate.
l.t~ 29~
Example 1 Four tests were carried out. 68 g. of toluene as solvent and 13.6 g. of monomers comprising 77% by weight butadiene and 23~ by weight styrene were introduced into 250 ml. Steinie bottles under nitrogen pressure. The catalyst system formed of LiAl(C2Hs)3~4Hg~and ~C2H5( 2 2 2 2 then added in the order indicated. The bottles were placed in a tank maintained thermostatically at 80C. in which they were agitated.
In Tests 2, 3 and 4, hydrogen was added during the course of the polymerization in such an amount that the amount of solubilized hydrogen was 1.5, 3 and 5 ppm., respectively. , At the end of 1 3/4 hours all the polymerization reactions were stopped by the addition of methanol and the copolymers were recovered in conventional manner.
The results are set forth in Table I and in Figs. 1.1-1.4.
The larger the amount of solubilized hydrogen, the lower the molecular weight of the low molecular weights.
- 20 Example 2 - Two tests were carried out. 68 g. of toluene as solvent and 17.6 g. of monomers comprising 25% by weight styrene and 75% by welght butadiene were introduced into 250 ml. Steinie bottles under nitrogen pressure.
The catalyst system formed of Ba~al(C2H5)472 and tetrahydrofuran (THF) was then added. The bottles were placed in a tank maintained thermostatically at 80C. in which they were agitated.
In Test 2I hydrogen was added during the course of the polymerization in such an amount that the amount of solubilized hydrogen was 5 ppm.
At the end of two hours, all the polymerization ~ 2;~1 reactions were stopped by the addition of methanol and the copolymers were recovered in conventional manner.
The results are set forth in Table II and in Figs.
2.1-2.2.
EXample 3 Two tests were carried out. 68 g. of toluene as solvent and 17.5 g. of butadiene were introduced into 250 ml.
Steinie bottles under nitrogen pressure. The catalyst system formed of Ba~Al(C2H5)472 and lithium ethyl diglycolate -C2H5(OCH2CH2)2O Li - was then added. The bottles were placed in a tank maintained thermostatically at 70C. in which they . .
were agitated.
In Test 2, hydrogen was added during the course of the polymerization in such an amount that the amount of solubilized hydrogen was 5 ppm.
At the end of two hours, all the polymerization reactions were stopped by addition of methanol and the homopolymers were recovered in conventional manner.
The results are set forth in TabIe III and in ~lgs. ~ 3.2.
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As representative examples of vinyl aromatic com-pounds there are suitable, in particular, styrene, ortho-, meta- and para-methylstyrene, " vinyl toluene" , the di-and poly-methylstyrenes, p-tertiobutylstyrene, the vinyl naphthalenes, the methoxystyrenes, the halostyrenes, vinyl mesitylene and divinyl benzene.
The following nonllmitative examples are given by way of illustration of the invention. In these examples, the inherent viscosities are established at 25C. in a 1 g./liter solution in toluene; the concentrations of compounds constitut-ing the catalyst system are expressed in micromols per 100 g.
of monomers. The percentages of 1,2 and trans linkages are expressed with respect to the polybutadiene portion and the percentage of styrene is expressed with respect to the total amount of copolymer obtained.
The time elapsed between the start of the polymer-ization reaction and the moment when the modifying agent is added is designated ln the examples as " elapsed time" and the percentage of conversion reached at the time of the ad-dition of the modifying agent is designated by " % conv."
The figures of the drawing show the distribution of the molecular weights of the homopolymers obtained at the end of the polymerization reaction which was obtained by gel permeation chromatography. The molecular weights are shown on the abscissa and the refraction index difference ~i on the ordinate.
l.t~ 29~
Example 1 Four tests were carried out. 68 g. of toluene as solvent and 13.6 g. of monomers comprising 77% by weight butadiene and 23~ by weight styrene were introduced into 250 ml. Steinie bottles under nitrogen pressure. The catalyst system formed of LiAl(C2Hs)3~4Hg~and ~C2H5( 2 2 2 2 then added in the order indicated. The bottles were placed in a tank maintained thermostatically at 80C. in which they were agitated.
In Tests 2, 3 and 4, hydrogen was added during the course of the polymerization in such an amount that the amount of solubilized hydrogen was 1.5, 3 and 5 ppm., respectively. , At the end of 1 3/4 hours all the polymerization reactions were stopped by the addition of methanol and the copolymers were recovered in conventional manner.
The results are set forth in Table I and in Figs. 1.1-1.4.
The larger the amount of solubilized hydrogen, the lower the molecular weight of the low molecular weights.
- 20 Example 2 - Two tests were carried out. 68 g. of toluene as solvent and 17.6 g. of monomers comprising 25% by weight styrene and 75% by welght butadiene were introduced into 250 ml. Steinie bottles under nitrogen pressure.
The catalyst system formed of Ba~al(C2H5)472 and tetrahydrofuran (THF) was then added. The bottles were placed in a tank maintained thermostatically at 80C. in which they were agitated.
In Test 2I hydrogen was added during the course of the polymerization in such an amount that the amount of solubilized hydrogen was 5 ppm.
At the end of two hours, all the polymerization ~ 2;~1 reactions were stopped by the addition of methanol and the copolymers were recovered in conventional manner.
The results are set forth in Table II and in Figs.
2.1-2.2.
EXample 3 Two tests were carried out. 68 g. of toluene as solvent and 17.5 g. of butadiene were introduced into 250 ml.
Steinie bottles under nitrogen pressure. The catalyst system formed of Ba~Al(C2H5)472 and lithium ethyl diglycolate -C2H5(OCH2CH2)2O Li - was then added. The bottles were placed in a tank maintained thermostatically at 70C. in which they . .
were agitated.
In Test 2, hydrogen was added during the course of the polymerization in such an amount that the amount of solubilized hydrogen was 5 ppm.
At the end of two hours, all the polymerization reactions were stopped by addition of methanol and the homopolymers were recovered in conventional manner.
The results are set forth in TabIe III and in ~lgs. ~ 3.2.
.
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Claims (7)
1. A process of preparing a bimodal or multimodal homopolymer of a conjugated diene or a bimodal or multimodal copolymer of a conjugated diene with another conjugated diene or with a vinyl aromatic compound, consisting in polymerizing the monomer(s) in a reaction medium at a temper-ature of between 20°C. and 200°C. in the presence of a catalyst system formed of the reaction product of:
(a) an organic compound of a metal of group 3A
of the periodic classification of elements of the Mendeleev Table having one of the following formulas:
M2(M3R1R2R3R4)2 in which M1 represents an alkali metal, M2 represents an alkaline earth metal, M3 represents a metal of group 3A, R1, R2, R3 represent an alkyl or aralkyl radical and R4 represents either an alkyl or aralkyl radical or a radical XB in which X represents an oxygen, sulfur or nitrogen atom and B represents an alkyl or aralkyl radical or a radical M3(R5R6) in which R5, R6 represent an alkyl or aralkyl radical, with (b) at least one electron-donor compound containing at least one heteroatom selected from the group consisting of aprotic polar compounds, protic polar compounds and compounds formed of the reaction products of protic polar compounds with an alkali metal or with an alkaline earth metal, characterized by adding hydrogen as a modifying agent to the reaction medium during the course of the polymerization reaction.
(a) an organic compound of a metal of group 3A
of the periodic classification of elements of the Mendeleev Table having one of the following formulas:
M2(M3R1R2R3R4)2 in which M1 represents an alkali metal, M2 represents an alkaline earth metal, M3 represents a metal of group 3A, R1, R2, R3 represent an alkyl or aralkyl radical and R4 represents either an alkyl or aralkyl radical or a radical XB in which X represents an oxygen, sulfur or nitrogen atom and B represents an alkyl or aralkyl radical or a radical M3(R5R6) in which R5, R6 represent an alkyl or aralkyl radical, with (b) at least one electron-donor compound containing at least one heteroatom selected from the group consisting of aprotic polar compounds, protic polar compounds and compounds formed of the reaction products of protic polar compounds with an alkali metal or with an alkaline earth metal, characterized by adding hydrogen as a modifying agent to the reaction medium during the course of the polymerization reaction.
2. A process according to claim 1, characterized by the fact that the amount of hydrogen solubilized in the reaction medium is between 0.1 and 100 ppm.
3. A process according to claim 1 or 2, charac-terized by the fact that the catalyst system is formed of the reaction product of LiAl(C2H5)3C4H9 with [C2H5(OCH2CH2)2O]2Ba.
4. A process according to claim 1 or 2, charac-terized by the fact that the catalyst system is formed of the reaction product of Ba[Al(C2H5)4]2 with tetrahydrofuran.
5. A process according to claim 1 or 2, charac-terized by the fact that the catalyst is formed of the reaction product of Ba[Al(C2H5)4]2 with lithium ethyl diglycol-ate.
6. A process according to claim 1, characterized by the fact that the polymerization is conducted in a hydro-carbon solvent.
7. A process according to claim 6, characterized by the fact that the polymerization is conducted continuously.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR80-08110 | 1980-04-09 | ||
| FR8008110A FR2480289A1 (en) | 1980-04-09 | 1980-04-09 | PROCESS FOR THE PREPARATION OF POLYMERS OF CONJUGATED DIENES OR COPOLYMERS OF CONJUGATED DIENES EITHER THEREWITH OR WITH A COMPOUND |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1142291A true CA1142291A (en) | 1983-03-01 |
Family
ID=9240734
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000375137A Expired CA1142291A (en) | 1980-04-09 | 1981-04-09 | Process for preparing bimodal or multimodal polymers of conjugated dienes |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US4340703A (en) |
| EP (1) | EP0037618A1 (en) |
| JP (1) | JPS575706A (en) |
| AU (1) | AU540441B2 (en) |
| BR (1) | BR8102165A (en) |
| CA (1) | CA1142291A (en) |
| ES (1) | ES501186A0 (en) |
| FR (1) | FR2480289A1 (en) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5284811A (en) * | 1990-05-14 | 1994-02-08 | Phillips Petroleum Company | Polymerization catalysts and processes |
| US5151475A (en) * | 1991-04-15 | 1992-09-29 | Shell Oil Company | Termination of anionic polymerization |
| US5039755A (en) * | 1990-05-29 | 1991-08-13 | Shell Oil Company | Selective hydrogenation of conjugated diolefin polymers |
| US5141997A (en) * | 1990-08-15 | 1992-08-25 | Shell Oil Company | Selective hydrogenation of conjugated diolefin polymers |
| US5132372A (en) * | 1991-09-09 | 1992-07-21 | Shell Oil Company | Process for selective hydrogenation of conjugated diolefin polymers |
| US5206307A (en) * | 1991-09-09 | 1993-04-27 | Shell Oil Company | Process for selective hydrogenation of conjugated diolefin polymers |
| EP2679210B1 (en) | 2012-06-28 | 2015-01-28 | The Procter & Gamble Company | Absorbent articles with improved core |
| KR102106806B1 (en) * | 2018-02-09 | 2020-05-06 | 주식회사 엘지화학 | Method for preparing conjugated diene based polymer and apparatus for preparing conjugated diene based polymer |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2302311A1 (en) * | 1975-02-27 | 1976-09-24 | Michelin & Cie | PROCESS FOR PREPARING DIENE POLYMERS |
| US4112210A (en) * | 1975-02-27 | 1978-09-05 | Compagnie Generale Des Etablissements Michelin | Polymerization process |
| US4148985A (en) * | 1975-02-27 | 1979-04-10 | Compagnie Generale Des Etablissements Michelin | Polymerization process |
-
1980
- 1980-04-09 FR FR8008110A patent/FR2480289A1/en active Granted
-
1981
- 1981-04-03 JP JP5047281A patent/JPS575706A/en active Pending
- 1981-04-06 US US06/251,978 patent/US4340703A/en not_active Expired - Lifetime
- 1981-04-06 EP EP81200382A patent/EP0037618A1/en not_active Withdrawn
- 1981-04-08 ES ES501186A patent/ES501186A0/en active Granted
- 1981-04-09 CA CA000375137A patent/CA1142291A/en not_active Expired
- 1981-04-09 AU AU69333/81A patent/AU540441B2/en not_active Ceased
- 1981-04-09 BR BR8102165A patent/BR8102165A/en not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| ES8202567A1 (en) | 1982-02-01 |
| ES501186A0 (en) | 1982-02-01 |
| JPS575706A (en) | 1982-01-12 |
| FR2480289A1 (en) | 1981-10-16 |
| AU6933381A (en) | 1981-10-15 |
| FR2480289B1 (en) | 1985-05-03 |
| EP0037618A1 (en) | 1981-10-14 |
| US4340703A (en) | 1982-07-20 |
| AU540441B2 (en) | 1984-11-15 |
| BR8102165A (en) | 1981-10-13 |
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